Aminooxy-PEG3-azide - CAS 1306615-51-9

Aminooxy-PEG3-azide - CAS 1306615-51-9 Catalog number: BADC-00918

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Aminooxy-PEG3-azide is a non-cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Aminooxy-C2-PEG3-azide is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.

Category
ADCs Linker
Product Name
Aminooxy-PEG3-azide
CAS
1306615-51-9
Catalog Number
BADC-00918
Molecular Formula
C8H18N4O4
Molecular Weight
234.25
Aminooxy-PEG3-azide

Ordering Information

Catalog Number Size Price Quantity
BADC-00918 -- $--
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Description
Aminooxy-PEG3-azide is a non-cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Aminooxy-C2-PEG3-azide is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
Synonyms
O-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)hydroxylamine
IUPAC Name
O-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethyl]hydroxylamine
Canonical SMILES
C(COCCOCCOCCON)N=[N+]=[N-]
InChI
InChI=1S/C8H18N4O4/c9-12-11-1-2-13-3-4-14-5-6-15-7-8-16-10/h1-8,10H2
InChIKey
WSRXFPCTWIFEOF-UHFFFAOYSA-N
Solubility
10 mm in DMSO
LogP
0.38986
PSA
112.69000
Purity
≥98%
Shelf Life
0-4°C for short term (days to weeks), or -20°C for long term (months).
Shipping
Room temperature, or blue ice upon request.
Storage
Store at -5°C,keep in dry and avoid sunlight.

Aminooxy-PEG3-azide, a versatile chemical linker widely employed in bioconjugation and crosslinking, finds diverse applications in the following areas represented with heightened perplexity and burstiness:

Bioconjugation: Leveraging Aminooxy-PEG3-azide for bioconjugation purposes fosters the coupling of proteins, peptides, and other biomolecules with exceptional precision. This compound facilitates site-specific conjugation via oxime ligation, ensuring robust and effective attachment mechanisms. Such conjugations play a pivotal role in crafting targeted drug delivery systems and diagnostic tools, revolutionizing the realms of biomedicine.

Click Chemistry: Positioned as a cornerstone reagent in click chemistry, Aminooxy-PEG3-azide plays a pivotal role in catalyzing azide-alkyne cycloaddition reactions, particularly in the presence of copper. This dynamic enables the swift and selective formation of triazoles, expediting the synthesis of intricate molecules. Widely embraced in medicinal chemistry, material science, and nanotechnology, this technology drives innovation and complexity in various scientific domains.

Surface Modification: Unveiling its prowess in surface modification, Aminooxy-PEG3-azide emerges as a transformative tool for functionalizing diverse substrates like glass, nanoparticles, and polymers. By immobilizing biomolecules on these surfaces, researchers cultivate bioactive interfaces tailored for biosensors, bioassays, and tissue engineering endeavors. This breakthrough underscores significant progress in diagnostic platforms and biomedical devices, propelling the frontier of biotechnological advancements.

Drug Delivery: Within the realm of drug delivery, Aminooxy-PEG3-azide assumes a critical role in crafting drug conjugates and delivery vehicles engineered for precision and efficacy. The incorporation of the PEG linker enhances drug solubility and stability, while the azide group provides a platform for further functionalization. This strategic approach fortifies targeted drug delivery mechanisms, amplifying the therapeutic potential and efficacy of pharmaceutical agents.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Historical Records: Aminooxy-PEG3-azide
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